Canonical Allele Identifier: CA2306055684

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573283A= , CM000680.2:g.57573283A=	GRCh38
NC_000018.9:g.55240515A= , CM000680.1:g.55240515A=	GRCh37
NC_000018.8:g.53391513A=	NCBI36
NG_008175.1:g.18455T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.277T=	ENSP00000466263.1:p.Phe93=
ENST00000682485.1:n.389T=
ENST00000262093.11:c.277T= MANE Select	ENSP00000262093.6:p.Phe93=
ENST00000382873.8:c.61T=	ENSP00000372326.4:p.Phe21=
ENST00000651787.1:n.383T=
ENST00000652755.1:c.295T=	ENSP00000498358.1:p.Phe99=
ENST00000262093.9:c.277T=	ENSP00000262093.5:p.Phe93=
ENST00000382873.7:c.295T=	ENSP00000372326.3:p.Phe99=
ENST00000585494.5:c.277T=	ENSP00000465243.1:p.Phe93=
ENST00000585699.1:n.229T=
ENST00000585747.1:c.277T=	ENSP00000465717.1:p.Phe93=
ENST00000585878.1:n.329T=
ENST00000591215.5:c.61T=	ENSP00000467461.1:p.Phe21=
ENST00000592111.1:n.278T=
ENST00000592699.5:c.277T=	ENSP00000466263.1:p.Phe93=
NM_000140.3:c.277T=	NP_000131.2:p.Phe93=
NM_001012515.2:c.295T=	NP_001012533.1:p.Phe99=
XM_011525881.1:c.295T=	XP_011524183.1:p.Phe99=
XM_011525882.1:c.61T=	XP_011524184.1:p.Phe21=
NM_000140.4:c.277T=	NP_000131.2:p.Phe93=
NM_001012515.3:c.295T=	NP_001012533.1:p.Phe99=
XM_011525882.2:c.61T=	XP_011524184.1:p.Phe21=
XM_017025614.2:c.277T=	XP_016881103.1:p.Phe93=
NM_000140.5:c.277T= MANE Select	NP_000131.2:p.Phe93=
NM_001012515.4:c.295T=	NP_001012533.1:p.Phe99=
NM_001371094.1:c.277T=	NP_001358023.1:p.Phe93=
NM_001371095.1:c.61T=	NP_001358024.1:p.Phe21=
NM_001374778.1:c.277T=	NP_001361707.1:p.Phe93=